A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438902



Internal ID21096455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89016001..89017000hg38UCSC Ensembl
chr9:91630916..91631915hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187142
Samples
Known GenesSHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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